Alternative Targets for Modulators of Mitochondrial Potassium Channels

Mitochondrial potassium channels control potassium influx into the mitochondrial matrix and thus regulate mitochondrial membrane potential, volume, respiration, and synthesis of reactive oxygen species (ROS). It has been found that pharmacological activation of mitochondrial potassium channels during ischemia/reperfusion (I/R) injury activates cytoprotective mechanisms resulting in increased cell survival. In cancer cells, the inhibition of these channels leads to increased cell death. Therefore, mitochondrial potassium channels are intriguing targets for the development of new pharmacological strategies. In most cases, however, the substances that modulate the mitochondrial potassium channels have a few alternative targets in the cell. This may result in unexpected or unwanted effects induced by these compounds. In our review, we briefly present the various classes of mitochondrial potassium (mitoK) channels and describe the chemical compounds that modulate their activity. We also describe examples of the multidirectional activity of the activators and inhibitors of mitochondrial potassium channels.


Introduction
Earlier studies on isolated mitochondria have indicated that the transport of potassium ions is an important element in regulating their volume. This potassium transport process has also been observed in various cellular systems. Western blot analysis of isolated mitochondria has shown the presence of protein-binding antibodies specific to potassium channel counterparts in the plasma membrane. Finally, the presence of the mitoK channels in the inner mitochondrial membrane (IMM) was confirmed by measuring the activity of a single channel by the patch clamp technique. Mitochondrial potassium channels play an important role in mitochondrial functioning due to the flow of positive charge (in the form of K + ) through the IMM. These channel proteins have been identified in the mitochondria of various tissues, including the heart, skeletal muscle, and neuronal cells. Activation of mitoK channels by passing K + through the IMM causes changes in the mitochondrial membrane potential that increase mitochondrial oxygen consumption and influence mitochondrial ROS synthesis. Therefore, mitoK channels are an important part of cell signaling pathways and can be thought of as triggers for cell survival or cell death [1][2][3].
Several potassium channels have been identified in the IMM, such as ATP-sensitive potassium channels (mitoK ATP ); small (mitoSK Ca ), intermediate (mitoIK Ca ), and large conductance (mitoBK Ca ) calcium activated potassium channels; sodium dependent potassium (mitoSlo2) channels; and voltage-dependent (mitoKv1.3 and mitoKv7.4) potassium channels [4,5]. The activation of mitoK channels by means of small molecule potassium channel openers (KCOs) induces cardio-and neuroprotective effects against various injuries, including ischemia-reperfusion. On the other hand, the pharmacological inhibition of mitoKv channels induces cell death in cancer cells ( Figure 1) [1]. The beneficial effects induced by modulators of mitoK channels are related to changes in mitochondrial physiology. The activity of mitoK channels regulates the synthesis of mitochondrial ROS and mitochondrial matrix Ca 2+ uptake, which directly regulates the opening of the mitochondrial permeability transition pore (mPTP), a key trigger of cell death pathways [6]. openers (KCOs) induces cardio-and neuroprotective effects against various injuries, including ischemia-reperfusion. On the other hand, the pharmacological inhibition of mitoKv channels induces cell death in cancer cells ( Figure 1) [1]. The beneficial effects induced by modulators of mitoK channels are related to changes in mitochondrial physiology. The activity of mitoK channels regulates the synthesis of mitochondrial ROS and mitochondrial matrix Ca 2+ uptake, which directly regulates the opening of the mitochondrial permeability transition pore (mPTP), a key trigger of cell death pathways [6].
For these reasons, mitoK channels are promising targets for the development of new pharmacological tools to modulate their activity. However, the use of pharmacological modulators of mitoK channels carries a high risk that these compounds will interact with other targets in the cell, which can lead to unwanted effects or make it difficult to distinguish which effects are related to mitoK channels. In this review, we will provide basic information about the key modulators of mitoK channels and their alternative sites of action.

Modulators of Mitochondrial ATP-Sensitive Potassium Channels
The first potassium channel identified in the IMM was the ATP-sensitive potassium channel in rat livers [7]. This channel is inhibited by ATP and the antidiabetic sulfonylurea, glibenclamide [7]. Later, the same type of channel was identified in other tissues, such as the heart [8][9][10], brain [11][12][13], skeletal muscle [14], human T-lymphocytes [15], and skin fibroblasts [16]. Electrophysiological experiments revealed that the conductance of the channel is usually close to 100 pS [11,[17][18][19]; however, channels with For these reasons, mitoK channels are promising targets for the development of new pharmacological tools to modulate their activity. However, the use of pharmacological modulators of mitoK channels carries a high risk that these compounds will interact with other targets in the cell, which can lead to unwanted effects or make it difficult to distinguish which effects are related to mitoK channels. In this review, we will provide basic information about the key modulators of mitoK channels and their alternative sites of action.

Modulators of Mitochondrial ATP-Sensitive Potassium Channels
The first potassium channel identified in the IMM was the ATP-sensitive potassium channel in rat livers [7]. This channel is inhibited by ATP and the antidiabetic sulfonylurea, glibenclamide [7]. Later, the same type of channel was identified in other tissues, such as the heart [8][9][10], brain [11][12][13], skeletal muscle [14], human T-lymphocytes [15], and skin fibroblasts [16]. Electrophysiological experiments revealed that the conductance of the channel is usually close to 100 pS [11,[17][18][19]; however, channels with lower conductance, close to 10 pS, have also been reported [7,8]. These differences in reported conductance may result from the various experimental conditions. Initial findings suggested that the channel was formed by the Kir6.1 or Kir6. 2 subunits, yet the molecular identity of mitoK ATP remained unclear [20]. However, later studies showed that the ROMK2 isoform of the renal outer medullar potassium channel could be the structural component of the channel [9,21]. Interestingly, it was also suggested that the subunits of ATP synthase could form channels with mitoK ATP pharmacological properties [22]. Recently, it was shown that the pore-forming subunit of the mitoK ATP channel is a product of the CCDC51 gene [10]. Many studies have demonstrated that mitoK ATP is inhibited by glibenclamide; therefore, it was speculated that the SUR subunit, which is a glibenclamide receptor, is an integral part of the channel. Indeed, CCDC51 interacts with mitoSUR, encoded by the ABCB8 gene. The channel formed by these two proteins has the canonical pharmacological properties of the mitoK ATP channel [10]. Activation of the mitoK ATP channel induces or mediates cardio-or neuroprotection against various insults, including I/R. This phenomenon is well documented; however, the details of the cytoprotection mechanism are still not fully understood [17,23,24].
The list of pharmacological modulators of the mitoK ATP channel is relatively long. Diazoxide and BMS191095 can be treated as canonical pharmacological activators of the mitoK ATP channel [25], along with nicorandil, cromakalim, pinacidil, or P1075. Inhibitors of the mitoK ATP channel include glibenclamide (glyburide), 5-hydroxydecanoic acid (5-HD), tetraphenylphosphonium, and 4-aminopyridine [1,25]. 5-HD is described as a relatively selective inhibitor of mitoK ATP channels, and it does not inhibit plasma membrane K ATP channels [6,23]. However, all these compounds either have well-described alternative targets in the cell or induce cellular processes, which makes it difficult to reliably assess the detailed mechanism of their operation [26]. Importantly, most of these compounds were tested in the mitochondrial context.
The most notable opener of mitoK ATP channels is diazoxide, which is used in the treatment of diabetes [27]. Early studies revealed that this compound shows higher specificity toward mitoK ATP than to K ATP channels from the plasma membrane and sarcoplasmic reticulum [28]. Therefore, it is believed that the application of diazoxide at appropriately low concentrations should result in selective activation of the mitoK ATP channel. However, diazoxide inhibits the activity of respiratory chain complex II [29]. Moreover, diazoxide directly activates protein kinase c epsilon (PKC-ε) ( Table 1) [30]. Interestingly, it was shown that diazoxide and glibenclamide modulate the channel formed by CCDC51 only in the presence of the mitoSUR subunit [10]. Activation of ROMK2 found in mitochondria by diazoxide has also been observed [21].
Initial studies on isolated mitochondria suggested that BMS191095 was a specific activator of mitoK ATP channels [31,32] that activated the channels in the nanomolar range of concentrations [32]. Electrophysiological studies confirmed that this compound opens cardiac, neuronal, and dermal fibroblast mitoK ATP channels [11,16,33]. Several studies have shown that BMS191095 induces cytoprotection by activating mitoK ATP channels. For example, BMS191095 induced cytoprotection against I/R injury in mice and rat cardiac tissue [32,34] and pig skeletal muscle [35]; cytoprotection induced by this compound was reversed by 5-HD. Additionally, BMS191095 was shown to activate neuronal mitoK ATP , regulate neuronal mitochondrial function [36,37], and induce neuroprotection against various insults [36,38,39]. It was also shown that BMS191095 and the less-selective BMS180448 inhibited human platelet aggregation; preincubation with both glyburide and 5-HD blocked this effect [40]. In contrast, the application of BMS191095 protected myoblast C2C12 cells against toxicity induced by the deregulation of calcium homeostasis, and these effects were not reversed by 5-HD [41]. This compound was also shown to induce neurotoxicity effects [24,32].
Nicorandil, like diazoxide, was shown to mimic ischemic preconditioning of heart tissue by the activation of mitoK ATP channels [42,43]. However, this compound can also activate sarcolemmal K ATP channels [44]. Other studies have reported that nicorandil can be a donor of nitric oxide (NO) [45,46]. Additionally, it can stimulate superoxide dismutase and inhibit xanthine oxidase activity, therefore acting as an antioxidant [46][47][48]. The bidirectional effects of nicorandil were recently observed in a study describing the beneficial effects of this compound on fatigue in slow skeletal muscle fibers [43]. On the one hand, nicorandil activated the channel; on the other hand, it acted as an antioxidant and NO donor [43]. Further experiments revealed that nicorandil blocks mitochondrial glutamate malate-driven respiration in skeletal muscle [49]. Nicorandil can induce cytoprotection in dystrophin-deficient cardiomyocytes, and these effects are only partially reversed by the mitoK ATP blocker 5-HD [50]. Another recent example of the bidirectional activity of nicorandil can be seen in the regulation of the expression of selected genes, such as heme oxygenase-1 or interleukin-8, by nicorandil in human umbilical vein endothelial cells (HUVECs). Only some of the observed effects were reversed by 5-HD, and thus were linked to mitoK ATP activity [51]. In addition to the other openers listed above, it has also been suggested that malonate and atpenin A5, which are inhibitors of complex II, can activate mitoK ATP channels and induce cardioprotection [52,53].
Similar to mitoK ATP openers, inhibitors of this channel can either interact with other proteins or enter various metabolic pathways. For example, 5-HD, which is a canonical mitoK ATP inhibitor, was shown to inhibit sarcolemmal K ATP channels [54]. In contrast, 5-HD does not inhibit mitoK ATP from rat brains [11]. It was also found that 5-HD is metabolized by acyl-CoA synthetase and enters beta-oxidation, which can induce the switch from glucose to fatty acid metabolism [55][56][57]. Therefore, the direct interaction of 5-HD with mitoK ATP has been questioned. Additionally, 500 µM of 5-HD was shown to stimulate the activity of mitochondrial complex II and inhibit complex III in skeletal muscle cells [49]. Another study revealed that both glibenclamide and 5-HD can interact with ADP/ATP carriers from the inner mitochondrial membrane [58]. Additionally, glibenclamide can activate the mitochondrial permeability transition pore by increasing its sensitivity to calcium ions [59]. Moreover, glibenclamide inhibits chloride channels [60,61].
To examine whether the ROMK protein acts as a possible mitoK ATP channel-forming component, research has focused on the use of compounds regulating the activity of this protein. For example, it was reported that VU591 inhibits ROMK channels with high specificity [62][63][64]. However, this molecule induced mitochondrial depolarization and matrix contraction in mitochondria from both wild-type and ROMK knockout cells. [65]. Moreover, VU591 reversed matrix swelling induced by BMS191095 in the ROMK knockout cells. These observations suggest that VU591 has some alternative targets in mitochondria [65].

Mitochondrial Calcium-Activated Potassium Channels
In the IMM, a group of calcium-activated potassium channels have been identified, namely large conductance K + (mitoBK Ca ) channels [66], intermediate conductance K + (mitoIK Ca ) channels [67], and small conductance K + (mitoSK Ca ) channels [68]. Their common property is regulation by calcium ions-their open probability increases in the presence of Ca 2+ [17]. This common activation mechanism may indicate that these proteins are activated under the same physiological conditions. However, these channels differ in terms of other regulatory mechanisms. In addition, a different spectrum of pharmacological substances regulates their activity.

Large Conductance Calcium-Activated Potassium Channels
The mitoBK Ca channel was originally identified in the mitochondria of LN229 glioma cells by the patch clamp technique. The recorded channel had a conductance of 295 pS measured in a 150 mM KCl bath and pipette solution [66]. Later, the channel was described in other tissues, including the heart [69], brain [70,71], skeletal muscle [72], endothelium [73], dermal fibroblasts [74], and pulmonary and kidney epithelial cells [75,76]. Interestingly, similar channels have been identified in the mitochondria of mammals, lower organisms, and plants [77][78][79][80].
The pore-forming α subunit of both the mitoBK Ca and the plasma membrane BK Ca channels is encoded by the KCNMA1 gene. The VEDEC isoform of the α subunit (the name comes from the amino acid sequence at the C-terminus of the protein) is targeted to cardiac mitochondria [81,82]. Recently, it was shown that transfection with a VEDEC-encoding plasmid results in mitoBK Ca channel activity in HEK293T cells [83].
Several synthetic modulators have been used to activate the mitoBK Ca channel [6,95]. Some of the first synthetic BK Ca channel activators used for mitoBK Ca channels were the benzimidazolone derivatives NS1619 and NS004 [69,96,97]. Interestingly, NS004 was also described as a cystic fibrosis transmembrane conductance regulator (CFTR) channel opener [98]. Application of NS1619 protects the heart tissue from I/R injury, and many studies have shown that this effect may be mediated by mitoBK Ca [69,82,99]. NS1619 acts by shifting the voltage-sensor of BK Ca channels toward the activated state, as the open probability is barely altered when the voltage sensing domain (VSD) is at rest [100,101]. Although NS1619 is a known mitoBK Ca channel opener, this compound has many effects unrelated to the channel. For example, it can induce nonselective ion transport across the inner mitochondrial membrane [102] and inhibit complexes of the respiratory chain [102,103]. Another study showed that NS1619 has oligomycin-like properties and inhibits mitochondrial ATP synthase. Additionally, NS1619 inhibits sarco/endoplasmic reticulum Ca 2+ -ATPase (SERCA) [104], and L-type calcium channels ( Figure 2) [105]. NS1619 also stimulates Ca 2+gated chloride currents in smooth muscle cells of the rabbit pulmonary artery [106]. BK Ca channel-independent immediate and delayed preconditioning of neuronal cells was also observed after the application of NS1619 [107,108]. NS11021, a biarylthiourea derivative, has a higher potency and selectivity as a BKCa channel opener than NS1619 [109]. Application of NS11021 shifts the voltage-activation curve of the channel to more negative potentials, and activation is independent of free Ca 2+ concentration [100,110,111]. NS11021 increases the open probability of BKCa channels by altering the gating kinetics without affecting the single-channel conductance. It also protects the heart from I/R injury via mitoBKCa channel activation [110]. Interestingly, NS11021-induced activation of mitoBKCa channels prevents cold-storage induced injury of kidney epithelial cells [75].
Although NS11021 was thought to be more specific than NS1619, it was later shown to induce mitochondrial depolarization in a sucrose medium in the absence of K + salt [112]. It was also found that NS11021 applied at higher concentrations (10-30 μM) can activate KV7.4 and have minor inhibitory effects on Kv7.2/7.3 channels. The same study showed that NS11021 is a positive modulator of α7 nicotinic acetylcholine receptors at concentrations of 10-30 μM [109].
Another set of mitoBKCa channel openers is CGS7181 and CGS7184. Mitoplast patch clamp recording has revealed that the mitoBKCa channel of glioma cells is activated by CGS7184 [113]. Application of this opener decreased ROS synthesis by brain mitochondria in a model of reversed electron flow, and this effect was reversed by mitoBKCa channel Figure 2. Scheme of the targets of mitoBK Ca openers NS1619, NS004, and CGS7184. The targets located in mitochondria, endoplasmic reticulum, and plasma membrane are shown. "+"-activation, "−"-inhibition. NS11021, a biarylthiourea derivative, has a higher potency and selectivity as a BK Ca channel opener than NS1619 [109]. Application of NS11021 shifts the voltage-activation curve of the channel to more negative potentials, and activation is independent of free Ca 2+ concentration [100,110,111]. NS11021 increases the open probability of BK Ca channels by altering the gating kinetics without affecting the single-channel conductance. It also protects the heart from I/R injury via mitoBK Ca channel activation [110]. Interestingly, NS11021-induced activation of mitoBK Ca channels prevents cold-storage induced injury of kidney epithelial cells [75].
Although NS11021 was thought to be more specific than NS1619, it was later shown to induce mitochondrial depolarization in a sucrose medium in the absence of K + salt [112]. It was also found that NS11021 applied at higher concentrations (10-30 µM) can activate K V 7.4 and have minor inhibitory effects on Kv7.2/7.3 channels. The same study showed that NS11021 is a positive modulator of α7 nicotinic acetylcholine receptors at concentrations of 10-30 µM [109].
Another set of mitoBK Ca channel openers is CGS7181 and CGS7184. Mitoplast patch clamp recording has revealed that the mitoBK Ca channel of glioma cells is activated by CGS7184 [113]. Application of this opener decreased ROS synthesis by brain mitochondria in a model of reversed electron flow, and this effect was reversed by mitoBK Ca channel inhibitors [114]. However, in contrast to the effects of NS1619, CGS7184 and its derivative CGS7181 induced cell death, an effect unrelated to mitoBK Ca channel activation [113,115]. CGS7184 can also directly activate ryanodine receptor (RyR2) calcium release [116]. Evidently, the modulation of alternative targets by these compounds may be responsible for the observed increase in cytosolic calcium ion concentration [95].
Interestingly, both CGS7184 and NS1619 show mitoBK Ca channel activation in single channel patch clamp technique measurements; however, they exert opposing effects on cells. CGS7184 has a cytotoxic effect while NS1619 is cytoprotective. Therefore, the cytotoxic outcome of CGS7184 must be related to the off-target effects of this compound. Conversely, in the case of NS1619, the off-target effect is synergistic to some extent, leading to cytoprotection, especially in I/R processes. One of the mechanisms of action that distinguishes these compounds is the different manner in which calcium ions are released from the endoplasmic reticulum. CGS7184 releases Ca 2+ by opening RyR2 channels, while NS1619 releases Ca 2+ through the inhibition of SERCA in a pH-dependent manner [117,118]. Opening of RyR2 channels by CGS7184 naturally activates SERCA by Ca 2+ , which leads to a significant increase in the consumption of intracellular ATP, while NS1619 causes inhibition of SERCA, reducing ATP consumption. NS1619 s inhibition of SERCA increases as pH decreases and is reversible. Notably, a drop in pH occurs during ischemia ( Figure 2).
Another interesting mitoBK Ca channel modulator is chlorzoxazone, which is an FDAapproved centrally acting muscle relaxant [119]. This compound produces a left shift in the activation curve of BK Ca channels, yet it does not affect the Ca 2+ -sensitivity of the channels during that process [119]. It was used to treat a patient with progressive cerebellar degeneration, who had a BK G354S mutation in the KCNMA1 gene [120]. Chlorzoxazone also activates SK Ca and IK Ca channels, and 30 µM chlorzoxazone suppresses voltage-dependent L-type Ca 2+ currents [119]. Another mitoBK Ca channel modulator is a synthetic inhibitor with a natural origin: diCl-DHAA (12,14-dichlorodehydroabietic acid). It was reported to reduce I/R in rat cardiac myocytes [121,122].
The mitoBK Ca channel is also activated by naturally occurring openers. Similar to the plasma membrane BK Ca channel, the mitoBK Ca channel is activated by the sex hormone 17-estradiol (17β-estradiol, EST). 17β -estradiol has been applied to the mitoBK Ca channels in vascular smooth muscle using the black lipid membrane technique or the ventricular mitoplasts of rats using patch clamp [94]. The activation of mitoBK Ca channels by 17β-estradiol requires the β1 subunit [123]. 17β-estradiol has been described as an L-type channel agonist that induces a rapid increase in intracellular calcium concentration through the potentiation of the channel and the activation of cascade signaling pathways, such as Src/ERK/CREB/Bcl-2 [124]. Another example of a naturally occurring mitoBK Ca channel modulator is naringenin, a plant-derived flavonoid found in a variety of fruits and herbs [125]. Naringenin has been found to induce cardioprotection by activating mitoBK Ca channels [126]. Recently, it was shown that naringenin also activates mitoBK Ca and mitoK ATP channels in skin fibroblasts [127]. Naringenin also has a stimulatory effect on BK Ca channels in the absence of the auxiliary β subunits of the channel, increasing the probability of channel opening [128]. The beneficial effects of naringenin have been described for many disorders, including cardiovascular, pulmonary, metabolic, and neurological issues [95]. When applied to NSC-34 neuronal cells, naringenin shifted the activation curve of the M-type K + current (Kv7.2, 7.3, and 7.5) to more negative potentials [128].
Iberiotoxin, a toxin from the red scorpion Buthus tamulus is 68% homologous to charybdotoxin; however, it does not block any other ChTX-sensitive K + channels [133,134]. Moreover, iberiotoxin can block the BK Ca channel in the presence of the auxiliary β1 subunit [135]. Interestingly, both charybdotoxin and iberiotoxin are inactive in the presence of the auxiliary β4 subunit [136,137].
Lastly, quinine is a compound from cinchona trees that has been found to inhibit BK Ca channel-caused K + uptake into isolated mitochondria. Quinine is also known to inhibit K V 2.2 and K2P18.1 channels [144]. Structural studies have shown that BK Ca channels possess a conserved heme-binding sequence motif. Hemin binds to the linkage segment between the RCK1 and RCK2 domains and induces conformational changes different than those induced by Ca 2+ [85]. It regulates the inactivation of the K + channel and N-type inactivation of Kv1.4 and Kv3.4 channels [145].

Intermediate Conductance Calcium-Activated Potassium Channels
Intermediate conductance calcium-activated potassium channels from the mitochondrial inner membrane show a conductance close to 27 pS and were identified for the first time in human colon cancer cells [67]. The pore-forming subunit of IK Ca channels from the plasma membrane has six transmembrane spanning regions (S1-S6), with the conducting pore located between S5 and S6. The gating is conferred upon Ca 2+ binding to calmodulin (CaM), which is constitutively bound to the C-terminus of each channel subunit [146,147]. It was shown that the activity of IK Ca channels in the mitochondria and plasma membrane influences oxidative phosphorylation in pancreatic ductal adenocarcinoma cells [148].
IK Ca channels are inhibited by clotrimazole [67,155,[167][168][169], which can also inhibit BK Ca channels [170]. Clotrimazole plays a role in the acute inhibition and chronic induction of human cytochrome P450-dependent enzymes, leading to liver damage. The second inhibitor of the channel, TRAM-34, is a clotrimazole-based derivative [67,148,155,171,172]. It is more selective for IK Ca channels than it is for K V , BK Ca , and SK Ca channels [173]. TRAM-34 decreased astrogliosis and microglial activation, and attenuated memory loss in an Alzheimer's disease mouse model [174].

Small Conductance Calcium-Activated Potassium Channels
In the inner mitochondrial membrane, small conductance calcium-activated potassium channels have also been identified [68]. The conductance of SK Ca channels is approximately 4-14 pS. The gating of these channels is conferred by Ca 2+ binding to calmodulin, which, as with in IK Ca channels, is constitutively bound to the C-terminus of each channel subunit [146,147]. The plasma membrane and mitochondrial SK Ca channels are activated by several compounds, such as 1-EBIO, DCEBIO, NS309, CyPPA, or riluzole [151,155,[175][176][177]. As mentioned above, these compounds can also activate IK Ca channels; however, not all of these compounds were used in mitoSK Ca /IK Ca channel studies. The activation of the mitoSK Ca channel with NS309 is known to reduce neurotoxicity [151]. NS309 is a more potent activator of the recombinant SK2 channels than DCEBIO and 1-EBIO [178]. It has also been shown that 1-EBIO activates CFTR channels [179]. CyPPA-mediated activation of the mitoSK2 channel leads to neuroprotection of HT-22 cells [177,180]. CyPPA can also inhibit melanogenesis by modulating the GSK3β/β-catenin/MITF pathway, as well as reduce nitric oxide release in microglia [181].
The mitoSK Ca channel is inhibited by a canonical SK Ca channel peptide blocker, apamin [151,155,182]. This inhibitor blocks SK Ca channels in concentrations ranging from pM to nM. Apamin is known to bind to the outer pore region of the SK Ca channel; however, it is membrane impermeable and can show off-target activity at higher concentrations. Apamin regulates gene expression in various signaling pathways [183]; for example, it downregulates or inhibits the expression of TNF-α, intracellular cell adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1, transforming growth factor (TGF)-β1, fibronectin, the NF-κB signaling pathway, and signal transducers and activators of transcription (STAT) in vitro, thereby inhibiting proinflammatory cytokines and type 2 helper (Th2) lymphocyte chemokines [184].
The mitoSK Ca channel, similar to its plasma membrane counterpart, can be blocked by several synthetic inhibitors, such as NS8593 or UCL1684 [182,185]. UCL1684 mimics the binding residues of the structural elements of a naturally occurring inhibitory neurotoxin: apamin. This compound displaces apamin binding and is considered a pore blocker, acting at the apamin binding site [186]. SK Ca channels are also blocked by chlorzoxazone [187][188][189]. This compound, which serves as a muscle-relaxing drug and a probe for human liver cytochrome P-450IIE1 (CYP2E1), suppresses voltage-dependent L-type Ca 2+ current.

Mitochondrial Voltage-Dependent Potassium Channels
In the inner mitochondrial membrane, voltage-gated potassium channels, including mitoKv1.3, mitoKv1.5, and mitoKv7.4, have been identified [1]. These channels have also been found in the plasma membrane. Interestingly, the Kv1.3 channel is also present in the endoplasmic reticulum and the Golgi apparatus. The activity of Kv channels is regulated by changes in the cell membrane potential [190]. These channels are composed of voltage-sensing and pore-forming α-subunits and auxiliary β-subunits that enable them to perform a wide variety of physiological functions [191]. Each α-subunit is composed of six transmembrane domains (S1-S6) with the S1-S4 transmembrane domains surrounding a central pore domain built of two S5-S6 helices. The four α-subunits link together to form the functional square-pore structure of the Kv channel [192]. Previous work has shown that mitoKv1.3 channels are highly overexpressed in cancer cells and immune cells, and that modulation of these channels is effective in the treatment of cancer [193]. There are many Kv channel modulators, and we will focus only on those modulators that have been described as acting on the Kv channels found in mitochondria. Most of these modulators also modulate Kv channels present in various cellular compartments with different specificity dependent on the concentration used.

Mitochondrial Kv1.3 and Kv1.5 Channels and Their Modulators
The pore-forming subunit of the Kv1.3 channel is encoded by the KCNA3 gene. The presence of mitoKv1.3 channels was originally observed in T cells [194]; however, mitoKv1.3 channels are also present in cancer cells, such as leukemia Jurkat T cells, prostate cancer PC-3 cells, and breast cancer MCF-7 cells [195]. The Kv1.3 channel is also found in the nuclear membrane of Jurkat T cells, MCF-7 cells, A549 lung cancer cells, and SNU-484 gastric cancer cells, as well as in human brain tissue [196]. The mitoKv1.5 channel has been found in the inner mitochondrial membrane of J774 macrophages [197].
Kv1.3 channels have been identified in mitochondria by incubating isolated mitochondria with plasma membrane Kv1.3 channel-specific inhibitors, such as margatoxin (MgTx) and Stichodactyla toxin (ShK). These compounds are effective in inducing hyperpolarization of the mitochondrial membrane [194]. The Kv1.3 and Kv1.5 channels of the plasma membrane play a key role in the regulation of cell proliferation, migration, and differentiation; their inhibition leads to blockage of the cell cycle and cell proliferation [198]. In contrast, the inhibition of mitoKv1.3 and mitoKv1.5 channels, either by the Bax protein or by specific inhibitors, plays a key role in the activation of the apoptotic pathway [195,197]. Other known inhibitors of the mi-toKv1.3 channel are clofazimine and the non-phototoxic 5-methoxy-psoralen derivatives, Psora-4 and PAP-1 [199]. Application of MgTx, ShK, or Psora-4, results in changes in membrane potential, synthesis of reactive oxygen species (ROS), and release of cytochrome c from the mitochondrial intramembrane space [200]. Both MgTx and ShK act directly on the mitoKv1.3 channel when applied to mitoplasts. However, these inhibitors are peptides, which limits their permeation of cellular membranes; therefore, they are not useful as mitoKv1.3 channel inhibitors in vivo and in whole-cell studies. The peptide nature of these blockers also limits their ability to block channels in the plasma membrane, and their long-term administration carries the risk of provoking an immune response. This is not the case with psoralen derivatives, such as Psora-4 and PAP-1, and clofazimine, an antibacterial drug used in the treatment of leprosy (Table 3). Clofazimine inhibits the mitoKv1.3 and mitoKv1.5 channels, making it highly effective for studies on cancer treatment. In Vivo studies on the murine B16-F10 orthotopic melanoma model have demonstrated that the application of clofazimine resulted in a 90% reduction in tumor mass (Figure 3) [197]. In mice transplanted with orthotopic human COLO 357 cells, intraperitoneal administration of clofazimine resulted in a 50% reduction in tumor mass [201]. The use of clofazimine also led to apoptosis of B cells in patients suffering from chronic lymphocytic leukemia [199]. Additionally, clofazimine inhibits in vitro Wnt signaling in a wide range of triple-negative breast cancer subtypes that do not respond to hormonal drugs and targeted therapies [202]. Clofazimine also has an immunosuppressive effect that results from the selective blocking of the Kv1.3 channel, which is involved in the proliferation and survival of T effector cells, and, therefore, is a good target for the treatment of autoimmune diseases. Blocking the Kv1.3 channel changes the amplitude and frequency of intracellular Ca 2+ oscillation and inhibits the calcineurin/nuclear factor of activated T-cells (NFAT) signaling pathway [203]. Clofazimine interacts with and eventually blocks Kv1.3 channels in a precise and state-dependent manner. It may block open Kv1.3 channels during long depolarizations or block inactivated channels once they have been opened by brief depolarizations. Clofazimine's mechanism of blocking plasma membrane Kv1.3 channels opens up its possibility for use in the treatment of autoimmune diseases, where the expression of these channels in immune cells is increased [204]. Clofazimine is also a promising drug for the treatment of cryptosporidiosis and nonviral diarrhea in children [205]. In addition, it was effective at preventing skin graft rejection in a mouse transplant model [203]. The use of clofazimine in the treatment of drug-resistant tuberculosis has also been described. The mechanism of action in this case is not entirely clear; however, most likely it acts on Mycobacterium tuberculosis as a pro-drug that is reduced by NADH dehydrogenase, releasing reactive oxygen species upon reoxidation. Clofazimine likely competes with menaquinone (MK-4), a key cofactor in the mycobacterial electron transfer chain, for reduction by NADH [206].
Psora-4 has been shown to bind to the central, highly-conserved pore of Kv channels, and it may also bind to the side pockets formed by the backsides of the S5 and S6 helices In mice transplanted with orthotopic human COLO 357 cells, intraperitoneal administration of clofazimine resulted in a 50% reduction in tumor mass [201]. The use of clofazimine also led to apoptosis of B cells in patients suffering from chronic lymphocytic leukemia [199]. Additionally, clofazimine inhibits in vitro Wnt signaling in a wide range of triple-negative breast cancer subtypes that do not respond to hormonal drugs and targeted therapies [202]. Clofazimine also has an immunosuppressive effect that results from the selective blocking of the Kv1.3 channel, which is involved in the proliferation and survival of T effector cells, and, therefore, is a good target for the treatment of autoimmune diseases. Blocking the Kv1.3 channel changes the amplitude and frequency of intracellular Ca 2+ oscillation and inhibits the calcineurin/nuclear factor of activated T-cells (NFAT) signaling pathway [203]. Clofazimine interacts with and eventually blocks Kv1.3 channels in a precise and state-dependent manner. It may block open Kv1.3 channels during long depolarizations or block inactivated channels once they have been opened by brief depolarizations. Clofazimine's mechanism of blocking plasma membrane Kv1.3 channels opens up its possibility for use in the treatment of autoimmune diseases, where the expression of these channels in immune cells is increased [204]. Clofazimine is also a promising drug for the treatment of cryptosporidiosis and nonviral diarrhea in children [205]. In addition, it was effective at preventing skin graft rejection in a mouse transplant model [203]. The use of clofazimine in the treatment of drug-resistant tuberculosis has also been described. The mechanism of action in this case is not entirely clear; however, most likely it acts on Mycobacterium tuberculosis as a pro-drug that is reduced by NADH dehydrogenase, releasing reactive oxygen species upon reoxidation. Clofazimine likely competes with menaquinone (MK-4), a key cofactor in the mycobacterial electron transfer chain, for reduction by NADH [206].
Psora-4 has been shown to bind to the central, highly-conserved pore of Kv channels, and it may also bind to the side pockets formed by the backsides of the S5 and S6 helices and the S4-S5 linker [207]. The simultaneous occupation of both binding sites by the drug results in an extremely stable nonconducting state and increases Psora-4 selectivity for mitoKv1.3 and mitoKv1.5 channels [207]. Due to the inhibition of the plasma membrane Kv1.3 channel, Psora-4 can promote the differentiation and morphological, as well as electrophysiological, maturation of neurons derived from progenitor cells; therefore, it can be used in the treatment of multiple sclerosis [208]. By inhibiting the Kv1.3 channel present on T cells and glomerular infiltrating macrophages, Psora-4 halts rapidly progressive glomerulonephritis and may also be used to treat other autoimmune diseases [209].
PAP-1-MHEG is a recently synthetized PAP-1 derivative that has a higher degree of solubility due to the presence of an oligomeric chain of ethylene glycol. At a concentration of 10 µM, PAP-1-MHEG was able to induce apoptosis more effectively than could PAP-1 in cells isolated from leukemia patients that express mitoKv1.3. PAP-1-MHEG, similar to the other derivatives, blocks the mitoKv1.3 channel through the alkyl-O-phenyl part and causes depolarization of the mitochondrial membrane, which is crucial for the induction of apoptosis. It has also been found that the coumarin ring of PAP-1 and its derivatives acts as a "ROS generator" (Table 3) [210]. However, the unique aspect of PAP-1-MHEG is its ability to block the activity of respiratory chain complex I, via its the methoxy oligoethylene glycol (MOEG) domain, which may interfere with electron transport and the ubiquinone redox cycle. This interference is likely due to the proximity of the mitoKv1.3 channel and the NDUFS1 and NDUFS3 subunits of respiratory chain complex I; however, this requires further research [210]. None of the 5-methoxy-psoralen derivatives (Psora-4, PAP-1, PAPTP, PCARBTP, and PAP-1-MHEG) show any cytotoxic effect in cells with significantly fewer mitoKv1.3 channels, and do not significantly increase the mortality of tumor cells that overexpress mitoKv1.3 channels and have elevated ROS levels [199,210,211].

Mitochondrial Kv7.4 Channel and Its Modulators
The Kv7 channel subfamily consists of five members named sequentially from Kv7.1 to Kv7.5, encoded by the KCNQ1-5 genes. Each of these channels forms homotetramers, or sometimes heterotetramers, that exhibit different tissue distributions and physiological roles [212]. The Kv7.1 channel is present in the heart, pancreas, gastrointestinal tract, thyroid gland, brain, portal vein, and inner ear. The Kv7.2 and 7.3 channels are mainly expressed in the central nervous system; Kv7.4 is the major voltage-gated potassium channel in the inner ear and bladder smooth muscle; and Kv7.5 is expressed in skeletal muscle and plays a key role in contractility [213].
The presence of mitoKv7.4 channels was demonstrated in the mitochondria of H9c2 cardiomyoblasts and in isolated adult cardiomyocytes. This channel can be activated by retigabine and flupirtine, which induce mitochondrial depolarization and reduce the uptake of calcium ions into the matrix, resulting in cardioprotection against ischemia/reperfusion. This effect was abolished by the Kv7.4 channel inhibitor XE991 [214].
Both flupirtine and retigabine are activators of virtually all types of Kv7 channels, except Kv7.1, and thus have a broad spectrum of action and several side effects (Table 3).
Flupirtine is a triaminopyridine compound that serves as a nonopioid analgesic in the treatment of acute and chronic musculoskeletal pain [215]. It also has muscle relaxant [216] and anticonvulsant properties [217]. Flupirtine activates Kv7.2 and Kv7.3 channels, thus inhibiting the firing of sustained neuronal action potentials. This inhibits the excitability of neurons and reduces the excitatory transmission of neurotransmitters [218].
Flupirtine also acts as an N-methyl-D-aspartate (NMDA) antagonist and can reverse the effects of NMDA receptors, which play a key role in learning, although flupirtine does not bind directly to them. Additionally, flupirtine normalizes the level of intracellular glutathione and increases the expression of the antiapoptotic protein Bcl-2 in neuronal cells exposed to prion proteins. This neuroprotective effect of flupirtine can be used in the treatment of prion diseases [219]. Flupirtine has also been studied in the treatment of tinnitus and overactive bladder [220]. Approximately 8-12% of bioavailable flupirtine in humans is eliminated as a derivative of mercapturic acid by conjugating glutathione with intermediate quinone diimine, which is believed to be responsible for the hepatotoxicity of flupirtine [221].
Retigabine (RTG), also known as ezogabine, is used as an anticonvulsant drug (Table 3) [222]. This potassium channel opener has been approved as an adjunct to treat drug-resistant partial seizures [223]. However, due to its low benefit-to-risk ratio, the use of retigabine was discontinued in 2017, at which time the search for safer and more effective alternatives commenced [212].
RTG binds to Kv7.2-5 channels (encoded by  in neurons near the channel gate, which stabilizes the open channel state. The amino acid residues of glycine (G) 301 and tryptophan (W) 236 are crucial for this binding. The absence of W236 in KCNQ1 (which encodes the Kv7.1 channel) explains the lack of RTG binding to that channel [224]. Retigabine and flupirtine have shown antinociceptive effects in a rat model of gout. It is believed that Kv7 channels generate low-threshold, inactivating voltage-gated potassium currents that play an important role in regulating the excitability of nociceptive neurons [225]. To date, the analgesic effect of RTG has been demonstrated in models of pain due to neuroplasticity, bone cancer [226], inflammation [227], nerve degeneration [228], and the application of capsaicin to the viscera [229]. RTG at high concentrations may also result in positive allosteric modulation of γ-aminobutyric acid (GABA) receptors, specifically GABAA, and affect GABA metabolism (at concentrations > 10 µM). At high concentrations (>100 µM) RTG may also be a weak inhibitor of sodium and calcium channels [230]. RTG and ethanol show a similar effect on GABAergic and glutamatergic neurotransmission, which suggests they may interact. RTG reduces the basal rate of dopamine release in a dose-dependent manner in the mesolimbic system, which may be important in the treatment of psychotic diseases [231]. In contrast to RTG, high doses of ethanol increase dopaminergic neurotransmission [232]. Repeated administration of RTG significantly reduces neurological changes in the hippocampus caused by long-term administration of ethanol [233]. RTG also reduces NMDA-induced cell apoptosis in organotypic hippocampal cultures and in models of hypoxia and hypoglycemia [234]. A reduction in memory impairment and a slight improvement in learning post-alcohol consumption were also observed in rats treated with RTG [235]. There are few other reports on the effects of RTG on memory; however, one study has shown that even a single administration of RTG immediately after a traumatic experience can prevent fear memory consolidation and thus prevent posttraumatic stress disorder [236]. Retigabine has shown a sedative effect in studies of mania and bipolar disorder treatment [237]. It also significantly reduces the duration of in vitro myotonia, which causes excessive muscle stiffness, by activating K + currents during the sequences of action potentials [238]. After cerebral ischemia and reperfusion, there was a reduction in the area of cerebral infarction, tightening of tight connections between the cells of the blood vessel epithelium, reduced permeability of the blood-brain barrier, and reduced levels of MMP-2 and MMP-9 proteins in the ischemic area under the influence of RTG [239]. RTG and flupirtine, due to their oxidizing properties, reduced serum-induced ROS levels in neurons in the dentate gyrus; thus, they showed neuroprotective effects unrelated to the activity of Kv7 channels [234]. At high concentrations (>100 µM), retigabine inhibits Kv1-9 and Kv11 channels; at low concentrations (0.3-3 µM) it also inhibits the Kv2.1 channel. This inhibition is partially irreversible and may account for some of the undesirable effects of RTG application. The neuroprotective effect of RTG in neurons may result from the coordinated action of RTG on the Kv2.1 and Kv7 channels [240].

Psora-4 Inhibitor
Inhibitor of plasma membrane Kv1.3, promotes the differentiation and maturation of neurons.
Potentially effective in the treatment of cancer. [210,211] Clofazimine Inhibitor Inhibitor of the calcineurin/NFAT pathway, inhibitor of mycobacterial electron transfer chain.
Potentially effective in the treatment of cancer and autoimmune diseases, approved for treatment of leprosy and drug-resistant tuberculosis. [202,204,206,209]

Mitochondrial Sodium-Activated Potassium Channels
Sodium-activated potassium channels belonging to the Slo2 (K Na ) family have been identified in the mitochondria of cardiac tissue [241][242][243]. Two genes encode Slo2 channels in mammalian cells: KCNT2, which encodes Slo2.1 (also known as Slick) channels, and KCNT1, which encodes Slo2.2 (Slack) channels [244]. The conductance of the Slack channel was found to be approximately 180 pS, while Slick was found to be approximately 140 pS [244]. Structurally, a part of the pore domain and the transmembrane S6 segment of the Slack channel share similarities with Slo1 channels [245]. Interestingly, Slo2 channels can form calcium-sensitive channels after interaction with BK Ca channels [244]. The activity of both Slo2.1 and Slo2.2 channels is stimulated by sodium ions [244,246,247]. These channels are also activated by several pharmacological compounds, including bithionol, riluzole, loxapine, and niclosamide [244,247]. Slo2 channels are inhibited by compounds such as bepridil [246], clofilium [248], R56865 [246], and quinidine [244,247] (Table 4). It was found that the activation of mitochondrial Slo2 channels by bithionol induced thallium uptake into isolated mouse cardiac mitochondria as well as mitochondria of C. elegans [243]. The activity of mitoSlo2 channels is inhibited by bepridil. It has been proposed that these channels play an important role in cardioprotection, similar to mitoBK Ca and mitoK ATP channels [241][242][243]249]. Recently, using the black lipid membrane technique, sodium-activated potassium channels with a conductance of 150 pS were described in brain mitochondria [250]. Sodium ions have been shown to decrease complex I activity and increase complex IV activity in isolated mitochondria. These effects are accompanied by a slight decrease in mitochondrial ROS synthesis and an increase in mitochondrial membrane potential. It was suggested that these effects were related to the activity of the channel. However, no pharmacology specific to Slo2 channels was used in the study [250].
The modulators used to identify and describe mitoSlo2 channels have multiple targets in the cell. For example, bithionol inhibits several enzymes, such as mammalian mitochondrial glutamate dehydrogenase [251,252], human adenylyl cyclase [253], and Nacyl-phosphatidylethanolamine phospholipase D [254]. Bithionol also induces effects at the cellular level. For example, the application of bithionol induced apoptosis in ovarian cancer cells via cell cycle arrest, ROS generation, and inhibition of autotaxin [255,256]. Bithionol has been identified as an apoptosis-inducing photosensitizer for keratinocytes [257]. Its antiseptic and anthelminthic activities have also been studied, e.g., it inhibits the 3-oxoacyl acyl-carrier-protein reductase of Plasmodium falciparum and the large tumor antigen of polyomaviruses [258][259][260].
Another cardiac mitoSlo2 channel opener, bepridil, is a known calcium channel inhibitor (inhibiting channels such as L-type Ca 2+ channels) and is used as an antiarrhythmic drug [261]. Additionally, it was shown that bepridil modulates the activity of a few potassium channels. In HEK 293 cells, a low micromolar concentration of bepridil (2-5 µM) inhibited the slow component of cardiac delayed rectifier K + currents composed of KCNQ1/KCNE1 gene products in a concentration-dependent manner [262]. Additionally, bepridil and R56865 inhibited K ATP channels in guinea pig ventricular myocytes, with an estimated IC50 value of 10.5 µM for outward K ATP channel currents at a +60 mV holding potential and 6.6 µM for inward currents recorded at −60 mV [246]. Another study showed that 1-10 µM bepridil activated the mitoK ATP channels of cardiac mitochondria in guinea pigs and induced cardioprotection against ischemia/reperfusion injury [263].
Clofilium is another modulator of Slo2 channels. This inhibitor can modulate a broad spectrum of channels, including Slo3, Kv1.5 [264], and TASK-2 channels [265], as well as NMDA receptors [266]. NMDA inhibition was observed after the application of 0.1 µM of clofilium [266]. Clofilium can also induce apoptosis in human promyelocytic leukemia cells [267]. Although clofilium has not been used for mitoSlo2 channel modulation, it was shown to play a role in mitochondrial DNA (mtDNA) maintenance, which was detected by an increase in mtDNA copy number in C. elegans and in yeast. A similar effect was observed in POLG-deficient cultured human fibroblasts after the application of 0.5-2.5 µM clofilium [268]. It was concluded that the observed effects were unrelated to the inhibition of potassium channels and that clofilium has a new target in yeast and human cells [268]. Interestingly, the application of clofilium reduced hypoxia-induced neuronal cell death; however, the neuroprotective mechanisms were related to the inhibition of K + efflux [269]. Table 4. Examples of mitochondrial sodium-activated potassium channel modulators and their off-target activity.

Name
Function Example of Off-Target Activity Clinical Use Ref.

Bithionol Opener
Inhibition of mammalian mitochondrial glutamate dehydrogenase, human adenylyl cyclase, and N-acylphosphatidylethanolamine phospholipase D. Induces apoptosis of ovarian cancer cells. Apoptosis-inducing photosensitizer for keratinocytes.
Treatment of helminthic infection, inhibits 3-oxoacyl acylcarrier-protein reductase of Plasmodium falciparum and the large tumor antigen of polyomaviruses; inhibits host caspases and also reduces the detrimental effects of anthrax lethal toxin, diphtheria toxin, cholera toxin, Pseudomonas aeruginosa exotoxin A, Botulinum neurotoxin, ricin, and Zika.
Potentially useful for treatment of POLG-related diseases. [267,269,270]

Modulators of Mitochondrial TASK Channels
To date, 15 genes encoding a group of two-pore domain K + channels (K2P) have been identified in mammalian cells [159,271]. The synthesized proteins are distinguished by a unique subunit architecture with a molecular weight of approximately 70 kDa [270,272,273]. The group of K2P channels has been divided into 7 functional groups: TREK, TRAAK, TALK, TWIK, TASK, THIK, and TRESK. TREK (K2P 2, K2P 10) and TRAAK (K2P 4) activity is regulated by pressure, temperature, lipid environment, and the presence of volatile anesthetics. TALK (K2P 16, K2P 17) is activated in an alkaline environment or by the presence of NO, and TWIK (K2P 7, K2P 1, K2P 6) has weak rectifying properties. TASK (K2P 15, K2P 3, K2P 9) is inhibited in an acidic environment and activated by volatile anesthetics. THIK (K2P 12, K2P 13) is inhibited by halothane; lastly, TRESK (K2P 18) is activated by calcium ions. The structure of the K2P channel includes four transmembrane (4TM) domains, two re-entry pore loop (P) domains, two selectivity filters (SF), and intracellular amine and carboxyl terminals. K2P also includes a so-called cap structure, which plays a special role in its regulation [270]. Two identical K2P subunits form a single, central selective K + pore, although some K2P subunits may also form heterodimeric complexes in vivo, e.g., TASK-1 and TASK-3 subunits [274,275]. The 4TM domains of the K2P channel family mediate the background potassium currents observed in many cells of bioelectric excitable tissues, such as the heart, brain, muscles, and sensory organs. Interestingly, K2P channels open in the physiological voltage range of the cell membrane and are simultaneously regulated by a number of neurotransmitters and biochemical mediators. It should be noted that, while single functional channels do not have two pores in their structure, each α-subunit has two P domains in its base sequence, hence the name K2P (two-pore domain and not two-porous) channels [270]. The K2P channel family includes the TASK potassium channel subfamily, composed of TASK-1, TASK-3, and TASK-5 [276,277], all of which display K + outwardly rectifying currents that do not depend on membrane voltage. TASK-1 and TASK-3-mediated currents are highly sensitive to extracellular pH [277][278][279]. TASK-5 has no functional expression [280]. The TASK-3 channel (K 2P 9.1, KCNK9, 8q24) was discovered more than 20 years ago in the plasma membrane of mammalian cells. Since then, TASK-3 potassium channels have also been identified in the inner mitochondrial membrane (mitoTASK-3) of melanocytes, melanomas (WM35 and B16F10), and keratinocytes [6,[281][282][283]. The mitoTASK-3 channel was detected in the human keratinocyte HaCaT cell line, with a channel conductance of 83 pS at positive voltages and 12 pS at negative voltages in symmetric 150 mM KCl, as measured by the single-channel patch clamp technique. Lidocaine and an acidic pH (<6.2) have been shown to block channel activity. The mitoTASK-3 channel, similar to its plasma membrane version, is also sensitive to an acidic pH [282,283]. Silencing TASK-3 gene expression leads to changes in mitochondrial structure and induces apoptosis in human melanoma cells [284]. It seems particularly interesting that thus far, only the TASK-3 channel from the K2P channel group has been identified in the inner mitochondrial membrane. The apparent lack of other K2P channels in the IMM to date is all the more curious because, as mentioned above, TASK-3 and TASK-1 can form a functional heterodimer of potassium ion transporting channels [274,275]. This may be due to the tissue-specific localization of the TASK-1 and TASK-3 channels. TASK-3-like channels have been located in the mitochondria of the aldosterone-producing layer of the adrenal cortex zona glomerulosa cells [285]. It was shown that knockdown of the TASK-3 gene caused changes in migration and cell survival in gastric cancer, and that the TASK-3 gene could be a potential target for gastric cancer treatment; however, it was not possible to distinguish the role of mitoTASK-3 in addition to the plasma membrane isoform [286]. The role of mitochondrial potassium channels in cancer development was discussed in a recent review [287]. Studies have also shown that overexpression of TASK-3 channels occurs in several types of cancer, such as melanoma, ovarian carcinoma, and breast cancer [281,282,[288][289][290][291]. One of the major problems in distinguishing the role of mitochondrial potassium channels from those located in the plasma membrane is their molecular identity or close similarity. Nevertheless, despite the extensive structural similarity of K2P channels, there are differences in the interaction of small molecule compounds among these channels, which may also explain small structural differences as well as why only TASK-3 is located in the IMM [270]. Unfortunately, there are only a few known small-molecule compounds that modulate the activity of the TASK-3 channel [292]. To date, the verified modulators of TASK-3 channels include: the recently described plant-derived compound withaferin A (known in traditional medicine for centuries) [293], an inhibitor based on THPP (5,6,7,8-tetrahydropyrido [4,3-d]pyrimidine) [292] and its recently synthesized derivatives IN-THPP and mitoIN-THPP [294], ruthenium red (which has an IC50 of 0.7 µM) [295], and DR16 and DR16.1, which can penetrate biological membranes [276].
Recently, a study by Zúñiga et al. showed that withaferin A, the active biological component of Withania somnifera plant extract, has properties that inhibit the activity of the TASK-3 channel on the cell membrane (Table 5) [293]. In light of recent studies, this is an extremely interesting observation, as the expression of the KCNK9 gene for TASK-3 channels is increased in human breast tumors and lung tumors [295] and in 90% of ovarian tumors [288]. Despite the demonstration of a direct effect of withaferin A on the activity of the TASK-3 channel, it should be noted that it is still unclear whether it only affects the channel located in the plasma membrane or also that in the IMM. Withaferin A also acts on cellular pathways, such as cell cycle arrest [296,297], inhibits apoptosis via activated Akt-mediated inhibition of oxidative stress and ROS-dependent mitochondrial dysfunction in human colorectal cancer cells [298,299], and inhibits endoplasmic reticulum stress-associated apoptosis [300]. Low doses of withaferin A are cardioprotective in ischemia/reperfusion events via upregulation of the antiapoptotic mitochondrial pathway in an AMPK-dependent manner [301]. Another group of recently-synthetized inhibitors of TASK-3 channel activity is the 5,6,7,8-tetrahydropyrido [4,3-d]pyrimidine (THPP)-derived compounds IN-THPP and mitoIN-THPP, which differs by the addition of a triphenylphosphonium (TPP) group [294]. Because of its positive charge, the TPP group directs the mitoIN-THPP compound to the IMM. MitoIN-THPP is thus able to inhibit cancer cell migration to a higher extent than IN-THPP, which suggests that mitoTASK-3 is important in cell melanoma cell survival. It should be mentioned that after accumulation in the IMM, mitoIN-THPP is hydrolyzed to IN-THPP-COOH (the active molecule) and TPP-propyl-OH, which is itself unable to trigger apoptosis [292]. Ruthenium red and Ru360, other potential inhibitors of the TASK-3 potassium channel, are only useful for measurements in isolated TASK-3 channels systems because of their broad spectrum of interactions with different proteins in the cell, e.g., ryanodine receptors and mitochondrial calcium uniporter (MCU), respectively [302][303][304][305]. Because ruthenium red and Ru360 are known compounds that disturb intracellular calcium homeostasis, it is difficult to examine the role of TASK-3 and mitoTASK-3 in cellular processes [295,304,[306][307][308]. Two novel TASK-3 channel inhibitors (DR16 and DR16.1) were found using virtual screening, and their inhibitory potency was tested using the whole cell patch clamp technique. DR16 had an IC 50 of 56.8 µM, and DR16.1 had an IC 50 of 14.2 µM. DR16 and DR16.1 also have inhibitory potency for the TASK-1 channel, with an IC 50 of 24.7 µM and IC 50 of 21.21 µM, respectively [276]. It is worth noting that these compounds are not able to distinguish between TASK-1 and TASK-3, nor between those located in the plasma membrane and IMM.

Pharmacology of Mitochondrial HCN Channels
Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels are nonselective cation channels encoded by four genes, HCN-1,-2,-3, and -4, located on chromosomes 5, 19, 1, and 15, respectively, in humans. HCN channels belong to the superfamily of channels with six transmembrane segments [311]. Functional channels result from the assembly of four subunits, which together form a centralized pore that regulates ion flow across the membrane. Each subunit has several domains: a transmembrane voltage-sensing domain, a transmembrane pore-forming domain, a cytoplasmic C-linker, and a cytoplasmic cyclic nucleotide-binding domain (CNBD), which is critical for the modulation of the channels by cyclic nucleotides [312,313]. HCN channels also have an auxiliary TRIP8b subunit (Rab8b-interacting protein), which acts as an antagonist of cAMP. In the presence of TRIP8b, HCN channels only open at more hyperpolarized potentials [314]. The cryo-EM structures of the human HCN1 channel (hHCN1) have been determined in the absence and in the presence of cAMP, a physiological ligand of HCN channels [184].
HCN channels are mainly expressed throughout the heart and the central nervous system. HCN1 is highly expressed in the neocortex, hippocampus, cerebellar cortex, brainstem, and spinal cord. HCN2 is especially abundant in thalamic and brainstem nuclei. The expression of HCN3 is relatively modest, scattered throughout the brain. HCN4 is expressed in the olfactory bulb and the thalamus. All HCN subunits are expressed in the peripheral nervous system [315]. In the heart, all four isoforms have been detected and were differentially expressed according to the cardiac region. HCN2 and HCN4 are the most abundant isoforms in most mammalian atria and ventricles [316], which also display a minor presence of HCN1. HCN3 is expressed at a low level throughout cardiac regions. There is also evidence for the expression of HCN channels in cells outside of the nervous system and heart, such as the kidneys [317], pancreas [318], and bladder [319]. All HCN isoforms, except HCN3, are present in the retina [320]. HCN channels are localized mainly in the plasma membrane, although they have also been detected in the mitochondria of rat kidneys, human HEK 293 cells [321], and human cardiac tissue [321].
HCN channels are voltage-gated, and, in contrast to most other voltage-gated Kv channels, they are activated by membrane hyperpolarization [322]. HCN channels are permeable to both Na+ and K+ ions but are weakly selective for potassium compared with other voltage-gated Kv channels [323]. Functionally, they differ from each other in terms of activation time. HCN1 channels are the fastest; HCN4 channels are the slowest; and HCN2 and HCN3 are intermediate. In the case of physiological modulators, HCN channels are activated by direct binding of cyclic nucleotides, including cyclic monophosphate nucleotides, such as cAMP, cGMP, and cCMP. There is also evidence that HCN channels are regulated by changes in intracellular pH [155], cholesterol [324], phosphatidylinositol-4,5-bisphosphate [64], and caveolin 3 [33].
Dysfunction of HCN channels has been implicated in heart arrhythmogenic diseases and nervous system diseases, such as pain disorders, epilepsy, and ataxia [325][326][327]. Many pharmacological compounds influencing the activity of HCN channels affect not only the HCN channels of the cell membrane themselves, but also the mitochondrial HCN channels (Table 6). Unfortunately, some of them also have off-targets. One example is the bradycardic drug ZD7288. Experiments on isolated mitochondria showed that ZD7288 inhibits the flow of ions through HCN channels not only in the heart but also in the kidneys [321]. Additionally, ZD7288 was shown to reduce oxygen consumption coupled to ATP synthesis and hyperpolarization of the inner mitochondrial membrane [321]. ZD7288 may also directly block T-type Ca 2+ channels in mouse spermatogenic cells [328] and the sodium channel NaV1.4 in dorsal root ganglion [329], and can cause a robust depression of mossy fiber basal synaptic transmission [330]. Another HCN drug, ivabradine, also seems to be targeted to mitochondria. After ischemia/reperfusion mitochondrial stimulation, ivabradine reduced mitochondrial ROS formation and increased mitochondrial ATP production [331]. Ivabradine, a member of benzazepines, was the first clinically approved HCN channel blocker and is used to decrease heart rate. Ivabradine binds to the HCN channel pore and blocks HCN channels in pacemaker cells within the sinoatrial node; however, it is not specific to HCN isoforms. More specific to HCN channel isoforms are the modulators zatebradine and EC18 for HCN4 channels, MEL55A for HCN1 and HCN2 channels, and MEL57A for HCN1 channels. Additionally, another HCN channel modulator, gabapentin (an anesthetic, analgesic, and antiepileptic drug), reduces HCN4 channel-mediated currents in neurons [332] and inhibits mitochondrial branched-chain aminotransferase [333], opening mitochondrial ATP-dependent potassium channels and blocking voltage-gated calcium channels in a mouse model [334]. Lamotrigine, an HCN channel agonist (and anticonvulsant drug) may also block T-type Ca 2+ channels [335].

Summary and Perspectives
Over the last dozen years, emerging research on potassium channels clearly indicates their involvement in both protective processes and processes influencing cell death. It seems that one of the targets for the regulation of both cellular protection and apoptotic and necrotic processes is the potassium channels found in the inner mitochondrial membrane. A well-documented phenomenon is a protection of heart muscle cells from I/R injury with the use of small-molecule chemical compounds and potassium channel activators of the IMM, e.g., diazoxide and NS1619. Unfortunately, due to the presence of the same types of potassium channels in both the plasma membrane and the IMM, it is extremely difficult to distinguish their participation in both protective and cytotoxic processes. Additionally, the knockdown of the genes responsible for the expression of individual isoforms does not give the desired results, because potassium channels are usually expressed by the same genes, and the difference may result from alternative splicing. Small-molecule chemical compounds modulating the activity of the potassium ion channels in the plasma membrane also modulate the activity of those in the IMM. Although diazoxide acts through an auxiliary subunit, it exhibits the concentration differences necessary to activate a channel in the plasma membrane as well as that in the IMM. In light of recent studies, it seems extremely important to find ways to regulate the expression or activity of the channel only in the IMM, which could protect heart cells in the processes of ischemia/reperfusion or to induce apoptotic processes in cancer cells. Examining the side effects of small-molecule potassium channel modulators may also reveal synergistic pathways that regulate cytoprotection and cellular cytotoxicity, in addition to modulating potassium channels in the IMM.

Conflicts of Interest:
The authors declare no conflict of interest.